Cas 790300-29-7,Carbonic acid (Z)-(S)-4-cyclohexyl-4-hydroxy-but-2-enyl ester methyl ester

790300-29-7

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Basic information

Product Name: Carbonic acid (Z)-(S)-4-cyclohexyl-4-hydroxy-but-2-enyl ester methyl ester
Synonyms: Carbonic acid (Z)-(S)-4-cyclohexyl-4-hydroxy-but-2-enyl ester methyl ester
CAS NO:790300-29-7
Molecular Formula:
Molecular Weight: 228.288
EINECS: N/A
Product Categories: N/A
Mol File: 790300-29-7.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Carbonic acid (Z)-(S)-4-cyclohexyl-4-hydroxy-but-2-enyl ester methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbonic acid (Z)-(S)-4-cyclohexyl-4-hydroxy-but-2-enyl ester methyl ester(790300-29-7)
EPA Substance Registry System: Carbonic acid (Z)-(S)-4-cyclohexyl-4-hydroxy-but-2-enyl ester methyl ester(790300-29-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 790300-29-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 790300-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,3,0 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 790300-29:
(8*7)+(7*9)+(6*0)+(5*3)+(4*0)+(3*0)+(2*2)+(1*9)=147
147 % 10 = 7
So 790300-29-7 is a valid CAS Registry Number.

790300-29-7Upstream product

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790300-29-7Relevant articles and documents

An efficient, stereoselective approach to syn-1,2-diols protected as cyclic carbonates

Georges, Yohan,Allenbach, Yves,Ariza, Xavier,Campagne, Jean-Marc,Garcia, Jordi

, p. 7387 - 7390 (2007/10/03)

Enantioenriched 4-hydroxyalk-2-ynyl carbonates (or benzoates) have been prepared by stereoselective zinc-mediated addition of alkyl 2-propynyl carbonates (or their benzoate analogues) to aldehydes. Their partial reduction to Z-olefins followed by cyclizat

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